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NCT03499795 · ClinicalTrials.gov registry record · Phase 2

VGX-3100 Delivered Intramuscularly (IM) Followed by Electroporation (EP) for the Treatment of HPV-16 and/or HPV-18 Related Anal or Anal/Peri-Anal, High Grade Squamous Intraepithelial Lesion (HSIL) in Individuals Seronegative for Human Immunodeficiency Virus (HIV)-1/2

A Phase 2 study, sponsored by Inovio Pharmaceuticals.

Completed
Registry status
Phase 2
Development phase
23
Enrollment target

NCT03499795: Completed Phase 2 study, sponsored by Inovio Pharmaceuticals.

NCT03499795 is a Phase 2 study that has completed, run by Inovio Pharmaceuticals. The registered enrollment target is 23 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (83% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03499795, a Phase 2 study, has completed, sponsored by Inovio Pharmaceuticals.

COMPLETED
Registry status
Phase 2
Development phase
23 participants
Enrollment target

Study Summary

This is a phase 2, open-label efficacy study of VGX-3100 administered by intramuscular (IM) injection followed by electroporation (EP) in adult men and women who are human immunodeficiency virus (HIV) negative with histologically confirmed anal or anal/peri-anal high-grade squamous intraepithelial lesion (HSIL) associated with human papilloma virus (HPV)-16 and/or HPV-18. Approximately 24 participants will receive at least 3 doses of VGX-3100.

Interventions

  • BIOLOGICAL VGX-3100
  • DEVICE CELLECTRA™ 5PSP

Trial Details

FieldValue
Enrollment Target 23 participants
Start Date 2018-05-15
Est. Completion 2021-05-26
Phase Phase 2
Inovio Pharmaceuticals

28 total trials

What the finished NCT03499795 record still lists

NCT03499795 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 23 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (83% lower).

The record links to 0 conditions, and to 2 interventions - of which VGX-3100 is the first listed.

NCT03499795 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03499795 about?

NCT03499795 is a clinical study titled "VGX-3100 Delivered Intramuscularly (IM) Followed by Electroporation (EP) for the Treatment of HPV-16 and/or HPV-18 Related Anal or Anal/Peri-Anal, High Grade Squamous Intraepithelial Lesion (HSIL) in Individuals Seronegative for Human Immunodeficiency Virus (HIV)-1/2". This is a phase 2, open-label efficacy study of VGX-3100 administered by intramuscular (IM) injection followed by electroporation (EP) in adult men and women who are human immunodeficiency virus (HIV) negative with histologically confirmed anal or anal/peri-anal high-grade squamous intraepithelial l...

What is the current status of trial NCT03499795?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 23 participants. The study started on 2018-05-15. Estimated completion is 2021-05-26.

What interventions are being tested in trial NCT03499795?

The interventions under investigation include: VGX-3100 (BIOLOGICAL), CELLECTRA™ 5PSP (DEVICE).

Who is sponsoring clinical trial NCT03499795?

This trial is sponsored by Inovio Pharmaceuticals, which has 28 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03499795's enrollment target sits among peer trials

23 1784th of 2000 higher than 211 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT03499795, the US trial registry maintained by the National Library of Medicine. NCT03499795 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.